Meperidine Hydrochloride 00641-6052
Product NDC
00641-6052- Manufacturer
- Hikma Pharmaceuticals Usa Inc.
- Dosage Form
- Injection
- Route
- Intramuscular, Intravenous, And Subcutaneous
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- January 22, 1975
- Listing Expires
- December 31, 2026
- Application
- ANDA080445
Active Ingredients
| Ingredient | Strength |
|---|---|
| Meperidine Hydrochloride | 25 mg/mL |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
25 VIAL in 1 CARTON (0641-6052-25) / 1 mL in 1 VIAL (0641-6052-01)